Genetic sequencing for fetal structural problems
Part of Genetic & congenital clinical trials.
This study offers genetic sequencing to find the cause of certain serious fetal problems, such as structural anomalies, severe growth restriction, or unexplained pregnancy loss after 14 weeks. It aims to help families understand why the issue occurred and guide future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are at least 18 years old and pregnant
- Your fetus is found to have a structural problem, unexplained death after 14 weeks, severe growth restriction, or too much amniotic fluid
- You agree to have diagnostic testing such as karyotype or microarray
- The fetal problem is not already explained by a virus or a known chromosome change
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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